February 2026 Town Hall – Through Their Eyes: A Q&A Panel of Young Adults Living with JM

Feb 2026 Town Hall

Our February Town Hall featured a conversation designed for parents, grandparents, and caregivers navigating life with Juvenile Myositis. A small panel of young adults in their 20s who grew up with JM shared honest reflections on what they wish parents understood, what helped them most, and what—despite good intentions—made things harder along the way. Rather than offering a roadmap or one-size-fits-all answers, this discussion invited families to listen, reflect, and better understand the lived experience of JM through the voices of those who have walked it into adulthood.

Cure JM January 2025 – Virtual Summit

In January, the Cure JM Clinical Care Network was pleased to invite juvenile dermatomyositis healthcare professionals to join us virtually for the latest presentations from world-leading researchers and clinicians on advancements in basic research, translational studies, and best-practice clinical care in juvenile dermatomyositis. 

Family News

Family News

The Cure JM Foundation produces a monthly newsletter with the latest news and updates about juvenile myositis. Please click to read past issues of the Family News.

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